2-Amino-3-Iodo-5-Methylpyridine

≥98%

Reagent Code: #136211
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CAS Number 211308-79-1

science Other reagents with same CAS 211308-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.04 g/mol
Formula C₆H₇IN₂
badge Registry Numbers
MDL Number MFCD09037445
thermostat Physical Properties
Melting Point 86-89 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and antagonists. It serves as a building block in the production of drugs targeting neurological disorders such as Alzheimer's and Parkinson's diseases. Also employed in the preparation of agrochemicals, including certain herbicides and plant growth regulators. Its iodo functionality allows for further cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries during drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,120.00
inventory 5g
10-20 days ฿5,570.00
inventory 25g
10-20 days ฿27,430.00

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2-Amino-3-Iodo-5-Methylpyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and antagonists. It serves as a building block in the production of drugs targeting neurological disorders such as Alzheimer's and Parkinson's diseases. Also employed in the preparation of agrochemicals, including certain herbicides and plant growth regulators. Its iodo functionality allows for further cross-coupling reactions, making it valuable in medicinal chemistry for creati

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and antagonists. It serves as a building block in the production of drugs targeting neurological disorders such as Alzheimer's and Parkinson's diseases. Also employed in the preparation of agrochemicals, including certain herbicides and plant growth regulators. Its iodo functionality allows for further cross-coupling reactions, making it valuable in medicinal chemistry for creating diverse compound libraries during drug discovery.

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